Shankar P, Fabry J A, Fong D M, Lieberman J
Center for Blood Research, Harvard Medical School, Boston, MA 02115, USA.
Immunol Lett. 1996 Aug;52(1):23-30. doi: 10.1016/0165-2478(96)02574-6.
HIV-1 infection stimulates a strong CTL response that coincides with resolution of viremia in acute infection and declines with development of opportunistic infections. Recognition of HIV gp160 by PBMC-derived T cell lines from 20 HIV-infected subjects is dominated by the response to a small number of peptide epitopes. Overlapping CTL epitopes restricted by multiple MHC Class I elements were identified in 3 relatively conserved regions of gp160 (amino acids 49-68, 591-600 and 844-863). CTL from five of 20 subjects recognized three overlapping immunodominant epitopes in the 49-68 a.a. region restricted by A24, B38, and B55. CTL from four subjects recognized at least three distinct epitopes in a.a 591-600 in the context of A24, B8, B14, and B27. CTL from seven subjects recognized epitopes within a.a. 844-863 restricted by A30, B7, B8 and B35.
HIV-1感染会激发强烈的细胞毒性T淋巴细胞(CTL)反应,这种反应在急性感染期间与病毒血症的消退同时出现,并随着机会性感染的发展而下降。来自20名HIV感染受试者的外周血单核细胞(PBMC)衍生的T细胞系对HIV gp160的识别主要由对少数肽表位的反应主导。在gp160的3个相对保守区域(氨基酸49-68、591-600和844-863)中鉴定出受多种MHC I类分子限制的重叠CTL表位。20名受试者中有5名的CTL识别出49-68氨基酸区域中受A24、B38和B55限制的三个重叠免疫显性表位。4名受试者的CTL在A24、B8、B14和B27背景下识别出591-600氨基酸区域中至少三个不同的表位。7名受试者的CTL识别出844-863氨基酸区域内受A30、B7、B8和B35限制的表位。